Canonical Allele Identifier: PA2826319200
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 432062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230155.2:p.Ser355Arg
CA402701458
NM_001243226.3:c.1065C>G
CA402701459
NM_001243226.3:c.1065C>A
CA402701465
NM_001243226.3:c.1063A>C